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Browsing by Author Kalay, E.

Full Text	Issue Date	Title	Author(s)
	2011	CEP152 is a genome maintenance protein disrupted in Seckel syndrome	Kalay, E.; Yigit, G.; Aslan, Y.; Brown, K.E.; Pohl, E., et al
	2008	Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.	Collin, R.W.J.; Kalay, E.; Tariq, M.; Peters, T.A.; Zwaag, B. van der, et al
	2008	Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.	Ahmed, Z.M.; Masmoudi, S.; Kalay, E.; Belyantseva, I.A.; Mosrati, M.A., et al
	2007	MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation.	Kalay, E.; Uzumcu, A.; Krieger, E.; Caylan, R.; Uyguner, O., et al
	2007	Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.	Collin, R.W.J.; Kalay, E.; Oostrik, J.; Caylan, R.; Wollnik, B., et al
	2007	Variation of CNV distribution in five different ethnic populations.	White, S.J.; Vissers, L.E.L.M.; Geurts van Kessel, A.H.M.; Menezes, R.X. de; Kalay, E., et al
	2007	MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation.	Kalay, E.; Uzumcu, A.; Krieger, E.; Caylan, R.; Uyguner, O., et al
	2007	A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4.	Kalay, E.; Caylan, R.; Kiroglu, A.F.; Yasar, T.; Collin, R.W.J., et al
	2006	Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.	Kalay, E.; Li, Y.; Uzumcu, A.; Uyguner, O.; Collin, R.W.J., et al
	2005	A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein.	Wattenhofer, M.; Sahin-Calapoglu, N.; Andreasen, D.; Kalay, E.; Caylan, R., et al
	2005	GJB2 mutations in Turkish patients with ARNSHL: prevalence and two novel mutations.	Kalay, E.; Caylan, R.; Kremer, J.M.J.; Brouwer, A.P.M. de; Karaguzel, A.